Kaiyrzhanov, R., Rad, A., Lin, S.-J., Bertoli-Avella, A., Kallemeijn, W. W., Godwin, A., Zaki, M. S., Huang, K., Lau, T., Petree, C., Efthymiou, S., Karimiani, E. G., Hempel, M., Normand, E. A., Rudnik-Schöneborn, S., Schatz, U. A., Baggelaar, M. P., Ilyas, M., Sultan, T., … Maroofian, R. (2023). Bi-allelic ACBD6 variants lead to a neurodevelopmental syndrome with progressive and complex movement disorders. Brain, 147(4), 1436–1456. https://doi.org/10.1093/brain/awad380
Columbia Affiliation:
Subjects:
Peroxisome Proliferator-Activated Receptors
(OpenAlex Topic)
Ubiquitin-Proteasome Proteolytic Pathway
(OpenAlex Topic)
Endoplasmic Reticulum Stress and Unfolded Protein Response
(OpenAlex Topic)
Intellectual Disability
(MeSH)
Microcephaly
(MeSH)
Movement Disorders
(MeSH)
Nervous System Malformations
(MeSH)
Neurodevelopmental Disorders
(MeSH)
Publication Type:
Article
Unique ID:
10.1093/brain/awad380
PMID:
Journal:
Publication Date:
Data Source:
PubMed